Improving quality of life for older people with dementia and their caregivers
HAAL: HeAlthy Ageing Eco-system for peopLe With Dementia
This study is testing new technology to see if it can improve the quality of life for older people with dementia and make things easier for their caregivers.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 10 (estimated) |
| Ages | 65 Years and up |
| Sex | All |
| Sponsor | Istituto Nazionale di Ricovero e Cura per Anziani Academic / other |
| Locations | 1 site (Ancona) |
| Trial ID | NCT06307197 on ClinicalTrials.gov |
What this trial studies
The HAAL project aims to test various technological devices designed to enhance the quality of life for older adults with dementia and their caregivers. This feasibility study will assess the impact of these devices on caregiver stress, perceived quality of life, and overall cost-effectiveness compared to existing services. The study will be conducted in three locations: Italy, The Netherlands, and Taiwan, involving both informal and formal caregivers in its evaluation phases.
Who should consider this trial
Good fit: Ideal candidates for this study are caregivers of individuals with cognitive impairment or dementia who can commit to participating in the study.
Not a fit: Patients who do not have a caregiver or those unable to provide informed consent may not benefit from this study.
Why it matters
Potential benefit: If successful, this project could significantly improve the quality of life for individuals with dementia and reduce caregiver burden.
How similar studies have performed: While there have been studies focusing on technology for dementia care, the specific approach of the HAAL project is relatively novel and untested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * being the caregiver of a person with cognitive impairment or dementia; * availability of time to participate; * visit the assisted person at least two times at week or live with him/her. Exclusion Criteria: * Lack of written informed consent
Where this trial is running
Ancona
- IRCCS INRCA Hospital — Ancona, Italy (Recruiting)
Study contacts
- Study coordinator: Anna Rita Bonfigli
- Email: a.bonfigli@inrca.it
- Phone: 0718003719
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.